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Dentoskeletal Effects of the Expander With Differential Opening and the Fan-type Expander

Not Applicable
Completed
Conditions
Crossbite (Posterior)
Malocclusion
Interventions
Device: Differential Expansion
Device: Fan-Fype Expander
Registration Number
NCT03705871
Lead Sponsor
University of Sao Paulo
Brief Summary

This study will assess the dentoskeletal effects of two types of maxillary expanders in orthodontic patients in the mixed dentition, from 7 to 11 years old. Half of participants will be treated using the expander with differential opening, while the other half will undergo rapid maxillary expansion using the fan-type expander. The null hypothesis is that there is no difference between dentoskeletal effects of the two protocols.

Detailed Description

Rapid maxillary expansion (RME) is the orthopedic procedure of choice to treat maxillary constriction and posterior crossbite, and the study of dental, skeletal and periodontal effects of this procedure has been widely discussed in the orthodontic literature. The conventional RME expanders promote a similar expansion in the anterior and posterior regions of the maxillary arch. On the other hand, the fan-type expander allows the expansion concentrated in the intercanine region with little effects the intermolar distance. Finally, the expander with differential opening has two palatal screws and the differential activation protocol promotes a different amount of expansion for the anterior and posterior regions of the maxilla. No clinical study compared dental and skeletal effects of the expander with differential opening with those of the fan-type expander, including a three-dimensional analysis using CBCT exams and digital dental models. So, the aim of the present randomized clinical trial is to compare the skeletal and dentoalveolar effects of the maxillary expander with differential opening and the fan-type expander in the mixed dentition.

For this, patients will be recruited at the Orthodontic Clinic of Bauru Dental School, University of São Paulo, Brazil. A sample of 48 patients from 7 to 11 years old with transverse maxillary dental arch constriction will be prospectively and randomly allocated into two study groups. The first group will consist of 24 individuals treated with the expander with differential opening (DEG). The second group will consist of 24 individuals treated with the fan-type expander (FEG). In 12 patients from each group (immediate subgroups), a cone-beam computed tomography (CBCT) will be performed in the beginning of treatment (T1) and immediately after the rapid maxillary expansion (T2). In the other 24 patients, 12 from DEG and 12 from FEG (late subgroups), a CBCT will be obtained at T1 and 6 months after maxillary expansion (T3). Dental models will be obtained for all patients at T1 and T3. In digital dental models, maxillary arch width, perimeter, length and shape will be assessed. Standardized CBCT coronal sections will be used for measuring maxillary transverse dimensions, nasal cavity width and posterior tooth inclinations. Segmentation and superimposition of T1 and T3 CBCT images at the cranial base will be also performed. The opening of the midpalatal suture at the anterior and posterior region and the geometry of the suture opening will be evaluated in axial reconstructions of the CBCT.Discomfort, pain and quality of life will be evaluated by questionnaires.

After the normality test, the paired t test will be used in the intragroup comparison, and the independent t test will be used in the intergroup comparison. In the case of lost to follow-up patients, intention to treat analysis will be used. A significance level of 5% will be regarded for all tests.

Possible harms that could appear are related to temporary discomfort during the first days after the installation of the expander. Patients and legal guardians will be carefully oriented and they will be able to stop the treatment at any moment.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
48
Inclusion Criteria
  • Both sexes;
  • Mixed dentition;
  • Ages ranging from 7 to 11 years old;
  • Maxillary constriction associated to posterior crossbites;
  • Angle Class I or Angle Class II malocclusions.
Exclusion Criteria
  • Cleft lip and palate;
  • Craniofacial syndromes;
  • Carious lesions;
  • Angle Class III malocclusion;
  • History of previous orthodontic treatment.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Differential Expansion GroupDifferential ExpansionThe experimental group will be comprised 24 patients treated with a rapid maxillary expansion using the expander with differential opening. The expander is composed by two screws, one posteriorly and the other anteriorly positioned on the palate.
Fan-Fype Expander GroupFan-Fype ExpanderThe active comparator group will be comprised by 24 patients treated with rapid maxillary expansion using the the fan-type expander. The expander is composed by one screw anteriorly positioned on the palate.
Primary Outcome Measures
NameTimeMethod
Maxillary width (mm)6 months

Measurements will be performed in coronal sections of CBCT exams.

Maxillary deciduous canines inclination (°)6 months

Measurement be performed CBCT scans.

Opening of the midpalatal suture (mm)10 days

Measurement be assessed in axial and coronal sections of CBCT scans.

Maxillary and mandibular arch perimeter (mm)6 months

Measurements will be performed in digital dental models

Nasal cavity width (mm)6 months

Measurements will be performed in coronal sections of CBCT exams.

Maxillary and mandibular arch width (mm)6 months

Measurements will be performed in digital dental models

Maxillary and mandibular arch length6 months

Measurements will be performed in digital dental models

Maxillary molars inclination (°)6 months

Measurement will be performed in CBCT scans.

Amount of interincisor diastema (mm)10 days

Measurement will be assessed in CBCT scans.

Secondary Outcome Measures
NameTimeMethod
Quality of life evaluation using questionnaires6 months

The Child Perceptions Questionnaire (CPQ8-10) will be used to evaluate the quality of life of the patients before and after treatment.

Discomfort evaluation using questionnaires1 month

A Visual Analog Scale will be used from 0 to 10 cm.

Dentoskeletal displacements by three-dimensional superimposition of CBCT scams.6 months

Trial Locations

Locations (1)

Bauru Dental School - University of São Paulo

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Bauru, São Paulo, Brazil

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